Early Biomarker-Guided Prediction of Bloodstream Infection in Critically Ill Patients: C-Reactive Protein, Procalcitonin, and Leukocytes

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Early Biomarker-Guided Prediction of Bloodstream Infection in Critically Ill Patients : C-Reactive Protein, Procalcitonin, and Leukocytes. / Hertz, Frederik Boetius; Ahlström, Magnus G.; Bestle, Morten H.; Hein, Lars; Mohr, Thomas; Lundgren, Jens D.; Galle, Tina; Andersen, Mads Holmen; Murray, Daniel; Lindhardt, Anne; Itenov, Theis Skovsgaard; Jensen, Jens Ulrik Staehr.

In: Open Forum Infectious Diseases, Vol. 9, No. 10, ofac467, 2022.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Hertz, FB, Ahlström, MG, Bestle, MH, Hein, L, Mohr, T, Lundgren, JD, Galle, T, Andersen, MH, Murray, D, Lindhardt, A, Itenov, TS & Jensen, JUS 2022, 'Early Biomarker-Guided Prediction of Bloodstream Infection in Critically Ill Patients: C-Reactive Protein, Procalcitonin, and Leukocytes', Open Forum Infectious Diseases, vol. 9, no. 10, ofac467. https://doi.org/10.1093/ofid/ofac467

APA

Hertz, F. B., Ahlström, M. G., Bestle, M. H., Hein, L., Mohr, T., Lundgren, J. D., Galle, T., Andersen, M. H., Murray, D., Lindhardt, A., Itenov, T. S., & Jensen, J. U. S. (2022). Early Biomarker-Guided Prediction of Bloodstream Infection in Critically Ill Patients: C-Reactive Protein, Procalcitonin, and Leukocytes. Open Forum Infectious Diseases, 9(10), [ofac467]. https://doi.org/10.1093/ofid/ofac467

Vancouver

Hertz FB, Ahlström MG, Bestle MH, Hein L, Mohr T, Lundgren JD et al. Early Biomarker-Guided Prediction of Bloodstream Infection in Critically Ill Patients: C-Reactive Protein, Procalcitonin, and Leukocytes. Open Forum Infectious Diseases. 2022;9(10). ofac467. https://doi.org/10.1093/ofid/ofac467

Author

Hertz, Frederik Boetius ; Ahlström, Magnus G. ; Bestle, Morten H. ; Hein, Lars ; Mohr, Thomas ; Lundgren, Jens D. ; Galle, Tina ; Andersen, Mads Holmen ; Murray, Daniel ; Lindhardt, Anne ; Itenov, Theis Skovsgaard ; Jensen, Jens Ulrik Staehr. / Early Biomarker-Guided Prediction of Bloodstream Infection in Critically Ill Patients : C-Reactive Protein, Procalcitonin, and Leukocytes. In: Open Forum Infectious Diseases. 2022 ; Vol. 9, No. 10.

Bibtex

@article{1d61355cf0a2425c9178177c8fdc705b,
title = "Early Biomarker-Guided Prediction of Bloodstream Infection in Critically Ill Patients: C-Reactive Protein, Procalcitonin, and Leukocytes",
abstract = "Background: Bloodstream infections (BSIs) often lead to critical illness and death. The primary aim of this study was to determine the diagnostic accuracy of the biomarkers C-reactive protein (CRP), procalcitonin (PCT), and leukocyte count for the diagnosis of BSI in critically ill patients. Methods: This was a nested case-control study based on the Procalcitonin And Survival Study (PASS) trial (n = 1200). Patients who were admitted to the intensive care unit (ICU) <24 hours, and not expected to die within <24 hours, were recruited. For the current study, we included patients with a BSI within ±3 days of ICU admission and matched controls without a BSI in a 1:2 ratio. Diagnostic accuracy for BSI for the biomarkers on days 1, 2, and 3 of ICU admission was assessed. Sensitivity, specificity, and negative and positive predictive values were calculated for prespecified thresholds and for a data-driven cutoff. Results: In total, there were 525 patients (n = 175 cases, 350 controls). The fixed low threshold for all 3 biomarkers (CRP = 20 mg/L; leucocytes = 10 × 109/L; PCT = 0.4 ng/mL) resulted in negative predictive values on day 1: CRP = 0.91; 95% CI, 0.75-1.00; leukocyte = 0.75; 95% CI, 0.68-0.81; PCT = 0.91; 95% CI, 0.84-0.96). Combining the 3 biomarkers yielded similar results as PCT alone (P =. 5). Conclusions: CRP and PCT could in most cases rule out BSI in critically ill patients. As almost no patients had low CRP and ∼20% had low PCT, a low PCT could be used, along with other information, to guide clinical decisions. ",
keywords = "bloodstream infection, BSI, CRP, leukocyte, PCT",
author = "Hertz, {Frederik Boetius} and Ahlstr{\"o}m, {Magnus G.} and Bestle, {Morten H.} and Lars Hein and Thomas Mohr and Lundgren, {Jens D.} and Tina Galle and Andersen, {Mads Holmen} and Daniel Murray and Anne Lindhardt and Itenov, {Theis Skovsgaard} and Jensen, {Jens Ulrik Staehr}",
note = "Publisher Copyright: {\textcopyright} 2022 The Author(s). Published by Oxford University Press on behalf of Infectious Diseases Society of America.",
year = "2022",
doi = "10.1093/ofid/ofac467",
language = "English",
volume = "9",
journal = "Open Forum Infectious Diseases",
issn = "2328-8957",
publisher = "Oxford University Press",
number = "10",

}

RIS

TY - JOUR

T1 - Early Biomarker-Guided Prediction of Bloodstream Infection in Critically Ill Patients

T2 - C-Reactive Protein, Procalcitonin, and Leukocytes

AU - Hertz, Frederik Boetius

AU - Ahlström, Magnus G.

AU - Bestle, Morten H.

AU - Hein, Lars

AU - Mohr, Thomas

AU - Lundgren, Jens D.

AU - Galle, Tina

AU - Andersen, Mads Holmen

AU - Murray, Daniel

AU - Lindhardt, Anne

AU - Itenov, Theis Skovsgaard

AU - Jensen, Jens Ulrik Staehr

N1 - Publisher Copyright: © 2022 The Author(s). Published by Oxford University Press on behalf of Infectious Diseases Society of America.

PY - 2022

Y1 - 2022

N2 - Background: Bloodstream infections (BSIs) often lead to critical illness and death. The primary aim of this study was to determine the diagnostic accuracy of the biomarkers C-reactive protein (CRP), procalcitonin (PCT), and leukocyte count for the diagnosis of BSI in critically ill patients. Methods: This was a nested case-control study based on the Procalcitonin And Survival Study (PASS) trial (n = 1200). Patients who were admitted to the intensive care unit (ICU) <24 hours, and not expected to die within <24 hours, were recruited. For the current study, we included patients with a BSI within ±3 days of ICU admission and matched controls without a BSI in a 1:2 ratio. Diagnostic accuracy for BSI for the biomarkers on days 1, 2, and 3 of ICU admission was assessed. Sensitivity, specificity, and negative and positive predictive values were calculated for prespecified thresholds and for a data-driven cutoff. Results: In total, there were 525 patients (n = 175 cases, 350 controls). The fixed low threshold for all 3 biomarkers (CRP = 20 mg/L; leucocytes = 10 × 109/L; PCT = 0.4 ng/mL) resulted in negative predictive values on day 1: CRP = 0.91; 95% CI, 0.75-1.00; leukocyte = 0.75; 95% CI, 0.68-0.81; PCT = 0.91; 95% CI, 0.84-0.96). Combining the 3 biomarkers yielded similar results as PCT alone (P =. 5). Conclusions: CRP and PCT could in most cases rule out BSI in critically ill patients. As almost no patients had low CRP and ∼20% had low PCT, a low PCT could be used, along with other information, to guide clinical decisions.

AB - Background: Bloodstream infections (BSIs) often lead to critical illness and death. The primary aim of this study was to determine the diagnostic accuracy of the biomarkers C-reactive protein (CRP), procalcitonin (PCT), and leukocyte count for the diagnosis of BSI in critically ill patients. Methods: This was a nested case-control study based on the Procalcitonin And Survival Study (PASS) trial (n = 1200). Patients who were admitted to the intensive care unit (ICU) <24 hours, and not expected to die within <24 hours, were recruited. For the current study, we included patients with a BSI within ±3 days of ICU admission and matched controls without a BSI in a 1:2 ratio. Diagnostic accuracy for BSI for the biomarkers on days 1, 2, and 3 of ICU admission was assessed. Sensitivity, specificity, and negative and positive predictive values were calculated for prespecified thresholds and for a data-driven cutoff. Results: In total, there were 525 patients (n = 175 cases, 350 controls). The fixed low threshold for all 3 biomarkers (CRP = 20 mg/L; leucocytes = 10 × 109/L; PCT = 0.4 ng/mL) resulted in negative predictive values on day 1: CRP = 0.91; 95% CI, 0.75-1.00; leukocyte = 0.75; 95% CI, 0.68-0.81; PCT = 0.91; 95% CI, 0.84-0.96). Combining the 3 biomarkers yielded similar results as PCT alone (P =. 5). Conclusions: CRP and PCT could in most cases rule out BSI in critically ill patients. As almost no patients had low CRP and ∼20% had low PCT, a low PCT could be used, along with other information, to guide clinical decisions.

KW - bloodstream infection

KW - BSI

KW - CRP

KW - leukocyte

KW - PCT

U2 - 10.1093/ofid/ofac467

DO - 10.1093/ofid/ofac467

M3 - Journal article

C2 - 36225739

AN - SCOPUS:85145099952

VL - 9

JO - Open Forum Infectious Diseases

JF - Open Forum Infectious Diseases

SN - 2328-8957

IS - 10

M1 - ofac467

ER -

ID: 335055154